Mechanism and evolution of DNA primases

被引:111
作者
Kuchta, Robert D. [1 ]
Stengel, Gudrun [1 ]
机构
[1] Univ Colorado, Dept Chem & Biochem, Boulder, CO 80309 USA
来源
BIOCHIMICA ET BIOPHYSICA ACTA-PROTEINS AND PROTEOMICS | 2010年 / 1804卷 / 05期
关键词
Primase; Polymerase; NTP; dNTP; Mechanism; Inhibition; Counting; Fidelity; Misincorporation; Initiation; VIRUS HELICASE-PRIMASE; POLYMERASE-ALPHA-PRIMASE; PRIMER SYNTHESIS; ESCHERICHIA-COLI; TEMPLATE RECOGNITION; INITIATION SITES; HETERODIMERIC PRIMASE; REPLICATION PROTEINS; SEQUENCE SPECIFICITY; CRYSTAL-STRUCTURE;
D O I
10.1016/j.bbapap.2009.06.011
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
070307 [化学生物学]; 071010 [生物化学与分子生物学];
摘要
DNA primase synthesizes short RNA primers that replicative polymerases further elongate in order to initiate the synthesis of all new DNA strands. Thus, primase owes its existence to the inability of DNA polymerases to initiate DNA synthesis starting with 2 dNTPs. Here, we discuss the evolutionary relationships between the different families of primases (viral, eubacterial, archael, and eukaryotic) and the catalytic mechanisms of these enzymes. This includes how they choose an initiation site, elongate the growing primer, and then only synthesize primers of defined length via an inherent ability to count. Finally, the low fidelity of primases along with the development of primase inhibitors is described. (C) 2009 Elsevier B.V. All rights reserved.
引用
收藏
页码:1180 / 1189
页数:10
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